Canonical Allele Identifier: CA475394565
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352170C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584699C>A , CM000673.2:g.67584699C>A GRCh38
NC_000011.9:g.67352170C>A , CM000673.1:g.67352170C>A GRCh37
NC_000011.8:g.67108746C>A NCBI36
NG_012075.1:g.6105C>A , LRG_723:g.6105C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.159C>A ENSP00000381604.1:p.Leu53=
ENST00000398606.10:c.159C>A MANE Select ENSP00000381607.3:p.Leu53=
ENST00000646888.1:c.52C>A ENSP00000494477.1:p.Pro18Thr
ENST00000398603.5:c.159C>A ENSP00000381604.1:p.Leu53=
ENST00000398606.7:c.159C>A ENSP00000381607.3:p.Leu53=
ENST00000489040.1:n.158C>A
ENST00000494593.1:n.589C>A
ENST00000498765.5:c.122C>A
NM_000852.3:c.159C>A , LRG_723t1:c.159C>A NP_000843.1:p.Leu53=
NM_000852.4:c.159C>A MANE Select NP_000843.1:p.Leu53=